- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04863976
Effects of Different Stretching Techniques on Extensibility, Strength and Range of Motion in Football Athletes
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Castilla Y León
-
Soria, Castilla Y León, Spain, 42004
- Recruiting
- Luis Ceballos Laita
-
Contact:
- Luis Ceballos Laita, Ph.D
- Phone Number: 975 12 91 00
- Email: luis.ceballos@uva.es
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Footbal athletes
- Limited range of motion in ely's test
Exclusion Criteria:
- Previous surgery in the lower limb
- Previous physiotherapy threatment in the thigh
- Stretching contraindications
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Dynamic stretching
|
Dynamic movements of the joints controlled by the quadriceps muscle (hip and knee)
|
Active Comparator: Passive stretching
|
passive stretching of the quadriceps muscle
|
Active Comparator: Self-stretching
|
Self-stretching of the quadriceps muscle
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Range of motion
Time Frame: Baseline
|
the examiners assess the shoulder range of motion with an universal goniometer the examiners assess the shoulder range of motion with an universal goniometer The examiners assess the hip flexion and extension range of motion with an universal goniometer |
Baseline
|
Range of motion
Time Frame: immediately after the intervention
|
the examiners assess the shoulder range of motion with an universal goniometer the examiners assess the shoulder range of motion with an universal goniometer The examiners assess the hip flexion and extension range of motion with an universal goniometer |
immediately after the intervention
|
Strength
Time Frame: Baseline
|
The examiners assess the hip flexion and extension strength with a hand-held dynamometer
|
Baseline
|
Strength
Time Frame: immediately after the intervention
|
The examiners assess the hip flexion and extension strength with a hand-held dynamometer
|
immediately after the intervention
|
Extensibility
Time Frame: Baseline
|
The examiners assess the extensibility of the quadriceps and hamstring tissues using a digital inclinometer
|
Baseline
|
Extensibility
Time Frame: immediately after the intervention
|
The examiners assess the extensibility of the quadriceps and hamstring tissues using a digital inclinometer
|
immediately after the intervention
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Luis Ceballos Laita, PhD, University of Valladolid
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- PI21 - 2213
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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